首页> 外国专利> Prepn. of L-(selenium-75)-seleno:methionine - by reaction of selenium-75 with methyl:lithium, followed by reaction with L-alpha-amino-gamma bromo:butyric acid

Prepn. of L-(selenium-75)-seleno:methionine - by reaction of selenium-75 with methyl:lithium, followed by reaction with L-alpha-amino-gamma bromo:butyric acid

机译:准备-硒75与甲基:锂反应,然后与L-α-氨基-γ-溴:丁酸反应,制备L-(硒75)-硒基:蛋氨酸

摘要

Prepn. of L-(75Se)-selenomethionine (I) of high specific activity in amts. up to 1 Curie comprises: (a) reaction of 75Se of corresp. activity with an eight-fold molar excess of ethereal OMeli soln. (based on Se) in a remote-controlled apparatus; and (b) reaction of the resultant Me75Seli (II) with an ethanolic soln of two equivs. of L-alpha-amino-gamma-bromo-butyric acid hydrobromide (III) at room temp. in the same appts. Both processes are carried out under Argon. USE/ADVANTAGE - (I) is a useful radiopharmaceutical used for depiction of the pancreas. The process may be carried out in small amts. of liquid and is simpler than prior-art processes as step (b) takes place at room temp. Isolation of (I) is easier than in previous processes
机译:准备ams中具有高比活性的L-(75Se)-硒代蛋氨酸(I)的合成。最多1个居里包括:(a)75Se对应的反应。醚性OMeli溶液摩尔摩尔过量八倍而产生活性。 (基于硒)在遥控设备中; (b)所得的Me75Seli(II)与两个当量的乙醇溶液反应。室温下制备L-α-氨基-γ-溴丁酸氢溴酸盐(III)。在相同的应用程序中。两种方法均在氩气下进行。使用/优势-(I)是用于描绘胰腺的有用放射性药物。该过程可以在小范围内进行。由于步骤(b)在室温下进行,因此比现有技术的方法更简单。 (I)的隔离比以前的过程更容易

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